Anti-Human /Mouse /Rat SEPT9 Polyclonal Antibody

This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA02811
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human SEPT9
Specificity Widely expressed. Isoforms are differentially expressed in testes, kidney, liver heart, spleen, brain, peripheral blood leukocytes, skeletal muscle and kidney. Specific isoforms appear to demonstrate tissue specificity. Isoform 5 is the most highly expressed in fetal tissue. Isoform 1 is detected in all tissues except the brain and thymus, while isoform 2, isoform 3, and isoform 4 are detected at low levels in approximately half of the fetal tissues.
Isotype IgG
Reacitivity Human ,Mouse ,Rat
Clone
Uniprot Q9UHD8
Concentration 0.2 mg/mL
Dilution IHC 1:15-1:50
Formulation
Application IHC,ELISA
Other Names AF17q25,Cell division control protein septin D1,KIAA0991,MLL septin like fusion protein,MLL septin-like fusion protein,MLL septin-like fusion protein MSF-A,MSF,MSF1,NAPB,Ov/Br septin,Ovarian/breast septin alpha,Ovarian/Breast septin,PNUTL4,SEPT9,SEPT9,SeptD1,Septin 9,Septin D1,Septin-9,SINT1
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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